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1.
Am J Physiol Endocrinol Metab ; 295(5): E1167-71, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-18812459

RESUMEN

The neurohypophysial hormone oxytocin (OT), synthesized in magnocellular paraventricular (PVN) and supraoptic (SON) nuclei, is well known for its effects in lactation. Our previous studies showed that central OT receptor (OTR) binding is increased during gestation and that blockade of central OTRs, specifically during mid-late gestation, causes a delay in OT release during suckling and reduces weight gain in pups, suggesting decreased milk delivery. In the present study, we tested whether central OTR blockade during late gestation disrupts the gestation-related plasticity in intrinsic membrane properties. Whole cell current-clamp recordings were performed in OT neurons from pregnant rats (19-22 days in gestation) that were infused with an OTR antagonist (OTA) or artificial cerebrospinal fluid (aCSF) and from virgin rats infused with aCSF into the third ventricle via an osmotic minipump beginning on days 12-14 of gestation. The amplitudes of both Ca(2+)-dependent afterhyperpolarizations (AHPs), an apamin-sensitive medium AHP (mAHP) and an apamin-insensitive slow AHP (sAHP), were significantly increased during late gestation in control pregnant animals. However, the amplitude of the sAHP from pregnant rats treated with the OTA was significantly smaller than that of pregnant control rats and similar to that of virgins. These results indicate that the diminished efficiency in lactation due to OTR blockade may be partly a result of an altered sAHP that would shape OT bursting. These findings suggest that central actions of OT during late gestation are necessary for programming the plasticity of at least some of the intrinsic membrane properties in OT neurons during lactation.


Asunto(s)
Hipotálamo Anterior/fisiología , Neuronas/fisiología , Receptores de Oxitocina/fisiología , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Animales , Apamina/farmacología , Electrofisiología , Femenino , Edad Gestacional , Hipotálamo Anterior/citología , Hipotálamo Anterior/efectos de los fármacos , Lactancia/fisiología , Potenciales de la Membrana/efectos de los fármacos , Potenciales de la Membrana/fisiología , Plasticidad Neuronal/efectos de los fármacos , Plasticidad Neuronal/fisiología , Neuronas/citología , Neuronas/efectos de los fármacos , Ornipresina/análogos & derivados , Ornipresina/farmacología , Oxitocina/antagonistas & inhibidores , Oxitocina/farmacología , Oxitocina/fisiología , Embarazo , Ratas , Receptores de Oxitocina/antagonistas & inhibidores , Vasopresinas/fisiología
2.
Exp Neurol ; 196(2): 210-23, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16157332

RESUMEN

The central and systemic release of oxytocin (OT) has been well documented during parturition and lactation. In preparation for the demands of these events, the magnocellular hypothalamic neurons of the central OT system undergo a variety of biochemical, molecular, electrophysiological, and anatomical adaptations during gestation. However, the mechanisms responsible for these changes have not been well established. A number of neurochemical mediators have been implicated in contributing to the plasticity in the OT magnocellular system during gestation, including ovarian hormones, as well as central neurotransmitters, such as glutamate, gamma-amino butyric acid (GABA), and central neurosteroids, e.g., allopregnanolone. In addition, several lines of evidence suggest that central OT release and subsequent OT receptor stimulation may contribute to adaptations of the OT system during gestation, and may be necessary for its subsequent functioning during lactation. Here, we review evidence for involvement of the neurochemical systems implicated in contributing to adaptations that occur in the OT system during the course of gestation.


Asunto(s)
Hipotálamo Anterior/citología , Plasticidad Neuronal , Neuronas/metabolismo , Neurotransmisores/metabolismo , Oxitocina/metabolismo , Embarazo/fisiología , Animales , Femenino , Lactancia/fisiología , Receptores de Oxitocina/fisiología , Factores de Tiempo
3.
J Neuroendocrinol ; 15(8): 743-8, 2003 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12834434

RESUMEN

There is evidence that the central oxytocin system is activated and undergoes reorganization before parturition. The present study was designed to determine the effects of central oxytocin receptor blockade during late gestation on parturition, pup growth, and oxytocin release during suckling. Female Sprague-Dawley rats were implanted on gestation day 12-14 with Alzet osmotic minipumps containing an oxytocin receptor antagonist (d(CH2)5, Tyr(Me)(2), Orn(8)-vasotocin; OT-X) or artificial cerebrospinal fluid (VEH), which was infused into the third cerebral ventricle. Pumps were removed within 24 h of parturition. Daily maternal body weight and food intake were monitored during gestation and lactation. The length of gestation, duration of parturition, pup number, litter weight and interbirth interval were recorded. Subsequently, pup number and litter weights were recorded daily until lactation day 10 or 11, when maternal and pup behaviour, and plasma oxytocin concentration before and during suckling were measured. Central oxytocin blockade had no effect on the timing of parturition, maternal behaviour, litter size, still births, or litter weights at birth. However, beginning on day 3 of lactation, average weights of litters of OT-X females were significantly lower than litters of VEH-treated females. Furthermore, while basal plasma oxytocin concentrations, oxytocin increases in response to suckling and dam/pup interactions did not differ between groups, a significant delay in suckling-induced systemic oxytocin release was observed in OT-X females. Finally, OT-X dams weighed less than VEH dams during the postpartum observation period, although food intakes were similar. These data suggest that central actions of oxytocin during late gestation are necessary for the normal timing of systemic release of oxytocin during suckling, normal pup weight gain, and maintenance of maternal body weight.


Asunto(s)
Conducta Materna/efectos de los fármacos , Oxitocina/análogos & derivados , Oxitocina/metabolismo , Receptores de Oxitocina/antagonistas & inhibidores , Receptores de Oxitocina/fisiología , Animales , Animales Lactantes , Conducta Animal/efectos de los fármacos , Peso Corporal/efectos de los fármacos , Ingestión de Alimentos/efectos de los fármacos , Femenino , Edad Gestacional , Lactancia , Oxitocina/farmacología , Parto/efectos de los fármacos , Ratas , Ratas Sprague-Dawley
4.
J Exp Biol ; 206(Pt 10): 1697-706, 2003 May.
Artículo en Inglés | MEDLINE | ID: mdl-12682101

RESUMEN

To better understand the full extent of the odorant detection capabilities of fish, we investigated the olfactory sensitivity of zebrafish to a monoamine and several polyamines using electrophysiological and activity-dependent labeling techniques. Electro-olfactogram (EOG) recording methods established the relative stimulatory effectiveness of these odorants as: spermine >> spermidine approximately agmatine > glutamine > putrescine >or= cadaverine >or= histamine > artificial freshwater. The detection threshold for the potent polyamines was approximately 1 micromol l(-1). Cross-adaptation experiments suggested that multiple receptors are involved in polyamine detection. Three observations indicated that polyamine signaling may involve a transduction cascade distinct from those used by either amino acids or bile salts. Like bile salts and the adenylate cyclase activator forskolin, but unlike amino acid odorants, polyamines failed to stimulate activity-dependent labeling of olfactory sensory neurons with the cation channel permeant probe agmatine, suggesting a signaling pathway different from that used by amino acid stimuli. Also supporting distinct amino acid and polyamine signaling pathways is the finding that altering phospholipase C activity with the inhibitor U-73122 significantly reduced amino acid-evoked responses, but had little effect on polyamine- (or bile salt-) evoked responses. Altering cyclic nucleotide-mediated signaling by adenylate cyclase activation with forskolin, which significantly reduced responses to bile salts, failed to attenuate polyamine responses, suggesting that polyamines and bile salts do not share a common transduction cascade. Collectively, these findings suggest that polyamines are a new class of olfactory stimuli transduced by a receptor-mediated, second messenger signaling pathway that is distinct from those used by amino acids or bile salts.


Asunto(s)
Poliaminas Biogénicas/análisis , Odorantes/análisis , Olfato/fisiología , Pez Cebra/fisiología , Adaptación Fisiológica , Animales , Poliaminas Biogénicas/farmacología , Colforsina/farmacología , Electrofisiología , Femenino , Masculino , Neuronas Receptoras Olfatorias/efectos de los fármacos , Neuronas Receptoras Olfatorias/fisiología , Sistemas de Mensajero Secundario , Transducción de Señal , Olfato/efectos de los fármacos
5.
Am J Primatol ; 55(2): 101-15, 2001 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11668528

RESUMEN

Behavioral patterns were quantified in seven heterosexual lesser bushbaby (Galago moholi) pairs during the estrous cycle to determine the relative significance of behavioral and nonbehavioral components of female sexuality in mate attraction. Increases in the occurrence of several male behaviors indicating female attractiveness were initiated during vaginal swelling when the female was sexually nonreceptive. Female behavioral estrus, as indicated by intromission, was confined to a portion of vaginal opening coinciding with proestrous and vaginal estrous smears. Female attractiveness was maintained for much of the period of vaginal opening, whereas female receptivity ended a day or two earlier than attractiveness. Female receptive and proceptive behaviors were not well defined or extensive, and few female behaviors exhibited significant changes during the cycle. Scent-marking behaviors, such as urine washes, and male grooms, were generally elevated outside the behavioral estrous period. In G. moholi, male sexual arousal appears to be elicited primarily by female attractiveness, while behavioral components of female sexuality appear to be less important in influencing mate attraction.


Asunto(s)
Estro , Galago/psicología , Conducta Sexual , Animales , Animales de Zoológico , Femenino , Galago/fisiología , Masculino , Atractivos Sexuales
6.
J Neurophysiol ; 82(6): 3160-7, 1999 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-10601449

RESUMEN

Although it is generally assumed that fish are capable of discriminating amino acid odorants on the basis of differences in side-chain structure, less is known about their ability to discriminate amino acids with modifications to alpha-carboxyl and alpha-amino groups. In this study, the ability of the zebrafish olfactory system to detect and presumably discriminate analogues of the basic amino acid Arg was assessed, by using cross-adaptation and activity-dependent labeling techniques. Electrophysiological recordings established that esterification (L-arginine methyl ester; AME) or deletion (agmatine or amino-4-guanidobutane; AGB) of the alpha-carboxyl group yielded odorants more potent than Arg, whereas deletion of the alpha-amino group (L-argininic acid; AA) yielded a less potent analogue. In cross-adaptation experiments, no test-competitor odorant combination yielded complete cross-adaptation, suggesting the detection of these Arg analogues by multiple odorant receptors (ORs) with partially nonoverlapping specificities. Activity-dependent immunocytochemical labeling of olfactory receptor neurons supported this conclusion. AGB, an ion-channel-permeant probe (and odorant), labeled 4.9 +/- 0.4% (n = 24) of sensory epithelium, whereas the addition of Arg, 1-ethylguanidine sulfate, L-alpha-amino-beta-guanidinopropionate, or AME to AGB resulted in a significant elevation of labeling (8-14%). This study provides evidence that the olfactory system has the potential to discriminate among amino acid odorants with modified alpha-carboxyl and alpha-amino groups.


Asunto(s)
Arginina/análogos & derivados , Arginina/farmacología , Discriminación en Psicología/fisiología , Neuronas Receptoras Olfatorias/fisiología , Olfato/fisiología , Adaptación Fisiológica/fisiología , Animales , Electrofisiología , Femenino , Procesamiento de Imagen Asistido por Computador , Inmunohistoquímica , Masculino , Odorantes , Relación Estructura-Actividad , Pez Cebra
7.
Horm Behav ; 32(2): 73-84, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9367715

RESUMEN

The effects of ovariectomy, estradiol-17beta, and progesterone on female sexuality were investigated in a prosimian primate, the lesser bushbaby (Galago moholi). Each of eight ovariectomized, adult bushbabies was pair-tested with a male partner in the absence of hormone treatment, during estradiol-17beta (E2) treatment (3.125 microg/0.1 ml), and during E2 + progesterone (0.125 mg/0.1 ml) treatment. Pretreatment females were sexually nonreceptive and nonattractive toward the males. In contrast, E2 treatment elicited vaginal opening, partial or complete epithelial cell cornification, and female receptivity in all females and elicited the complete mating repertoire in seven pairs. Progesterone treatment opposed the facilitatory effects of E2 by inhibiting female receptivity and epithelial cell cornification and inducing vaginal closure. Behaviors were quantified following changes in hormone treatment, vaginal physiology, and the presence or absence of intromission. Female attractiveness (male sexual arousal) was initiated during vaginal swelling and was maintained for the duration of vaginal opening, while female receptivity was manifested exclusively during the period of vaginal opening. Female proceptive behavior was mainly associated with the period of receptivity. This study provided evidence of a strict hormonal regulation of both behavioral and nonbehavioral aspects of female sexuality in a prosimian.


Asunto(s)
Copulación/efectos de los fármacos , Estradiol/farmacología , Estradiol/fisiología , Galago/fisiología , Animales , Femenino , Masculino , Ovariectomía , Progesterona/fisiología , Reproducción/efectos de los fármacos , Reproducción/fisiología , Atractivos Sexuales/fisiología , Espermatozoides , Vagina/fisiología , Frotis Vaginal
8.
J Reprod Fertil ; 107(2): 167-74, 1996 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-8882281

RESUMEN

Urinary hormone profiles, determined by means of radioimmunoassays, were aligned with changes in mating behaviour and vaginal morphology and cytology during the ovarian cycles of adult, female lesser bushbabies (Galago moholi), a prosimian species. Intromission occurred in all seven females, 2.0 +/- 1.1 days (mean +/- SEM, median = 0) after the occurrence of vaginal opening, and lasted for 4.1 +/- 0.7 days. Three females subsequently gave birth. Vaginal swelling and labial reddening were initiated at least 2.5 +/- 0.5 days before vaginal opening and lasted 10.4 +/- 0.9 days. Pro-oestrous and vaginal oestrous smears coincided with vaginal opening, specifically during the period of mating. Concentrations of immunoreactive oestradiol increased during the first few days of vaginal opening in one pregnant female and in the nonpregnant females, and coincided with mating. Concentrations of immunoreactive progesterone did not show any temporal pattern for either pregnant or nonpregnant females. Concentrations of immunoreactive testosterone were generally higher during vaginal swelling and opening than during the remainder of the cycle in one pregnant female, whereas in nonpregnant females, no specific temporal pattern was evident. In both pregnant and nonpregnant females, immunoreactive LH concentrations increased during the period of vaginal swelling and opening, while in nonpregnant females increases were also apparent after vaginal closure. The data reported here are preliminary, and further research is necessary to establish conclusively patterns of excreted hormones during the reproductive cycles of Galago moholi and in other prosimian species.


Asunto(s)
Galago/fisiología , Hormonas Esteroides Gonadales/fisiología , Hormona Luteinizante/fisiología , Reproducción/fisiología , Vagina/fisiología , Animales , Creatinina/orina , Estradiol/fisiología , Estradiol/orina , Femenino , Hormona Luteinizante/orina , Masculino , Embarazo , Progesterona/fisiología , Progesterona/orina , Testosterona/fisiología , Testosterona/orina , Vagina/anatomía & histología , Vagina/citología
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